A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053226



Internal ID19142445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:73381736..73434580hg38UCSC Ensembl
Innerchr13:73955873..74008717hg19UCSC Ensembl
Innerchr13:72853874..72906718hg18UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg3852845
hg1952845
hg1852845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530505
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053226
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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